Disease: Familial (FPAH) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs145047094
rs145047094
Entrez Id: 9049
Gene Symbol: AIP
AIP
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE Co-occurrence of <i>MEN1</i> p.Gly111fs and <i>AIP</i> p.Arg16His Variants in Familial MEN1 Phenotype. 29848728 2018